Trimetrexate Plus Leucovorin Calcium Rescue Versus Sulfamethoxazole-Trimethoprim in the Treatment of Pneumocystis Carinii Pneumonia (PCP) in Patients With AIDS
Pneumonia, Pneumocystis Carinii, HIV Infections
About this trial
This is an interventional treatment trial for Pneumonia, Pneumocystis Carinii focused on measuring Trimethoprim-Sulfamethoxazole Combination, Trimetrexate, AIDS-Related Opportunistic Infections, Pneumonia, Pneumocystis carinii, Infusions, Intravenous, Leucovorin, Drug Therapy, Combination, Administration, Oral, Acquired Immunodeficiency Syndrome, Antiprotozoal Agents, AIDS-Related Complex, Sulfamethoxazole-Trimethoprim
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: Acetaminophen 650 mg prescribed as necessary for temperature > 38.7 degrees C. Acetaminophen q4h should not be prescribed as a standing order for more than 48 hours. Prior Medication: Allowed: Zidovudine as long as such therapy is suspended prior to randomization and not reinstituted until therapy for the acute episode is completed. Prophylaxis for Pneumocystis carinii pneumonia (PCP). Unequivocal diagnosis of Pneumocystis carinii pneumonia (PCP) by morphologic confirmation of three or more typical P. carinii organisms in sputum, bronchoalveolar lavage fluid, or lung tissue obtained by transbronchial or open-lung biopsy within 3 days before or after randomization. If morphologic confirmation is not possible prior to therapy, patients may be randomized if the investigator believes there is a high suspicion of PCP based on clinical presentation. If morphologic diagnosis cannot be established within 6 days of randomization, the patient will be withdrawn from study therapy. Resting alveolar-arterial oxygen differences = or > 30 mm Hg on room air. Exclusion Criteria Patients with the following are excluded: Inability to have alveolar blood gas analysis on room air. Medically unable to receive a liter of intravenous fluid (5 percent dextrose in water) per 24 hours. This procedure is required in order to maintain blinding. Prior Medication: Excluded within 14 days of study entry: Systemic steroids exceeding physiological replacement. Other investigational drugs. Excluded within 6 weeks of study entry: Antiprotozoal regimen for this episode consisting of pentamidine, eflornithine, DFMO, or dapsone, for therapy of active Pneumocystis carinii pneumonia (PCP) History of Type I hypersensitivity (i.e., urticaria, angioedema, or anaphylaxis), exfoliative dermatitis, or other life-threatening reaction secondary to antibiotics containing sulfa, trimethoprim, or trimetrexate. History of life-threatening pentamidine toxicity. Requirement for treatment with agents that are known to be myelosuppressive or nephrotoxic during the period of acute Pneumocystis carinii pneumonia (PCP) therapy. Other drugs for the treatment or prevention of AIDS or Pneumocystis carinii pneumonia (PCP); disulcid; aspirin; acetaminophen q4h for more than 48 hours.
Sites / Locations
- Ucsf Aids Crs
- Rush Univ. Med. Ctr. ACTG CRS
- Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU
- Washington U CRS
- SUNY - Buffalo, Erie County Medical Ctr.
- Case CRS